Canonical Allele Identifier: CA410682054

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868231C>A (hg19) ; chr22:g.19880708C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880708C>A , CM000684.2:g.19880708C>A	GRCh38
NC_000022.10:g.19868231C>A , CM000684.1:g.19868231C>A	GRCh37
NC_000022.9:g.18248231C>A	NCBI36
NG_011835.1:g.66129G>T , LRG_417:g.66129G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1096G>T MANE Select	ENSP00000383365.1:p.Glu366Ter
ENST00000400518.5:c.1006G>T	ENSP00000383362.1:p.Glu336Ter
ENST00000400519.6:c.1093G>T	ENSP00000383363.1:p.Glu365Ter
ENST00000400521.6:c.1096G>T	ENSP00000383365.1:p.Glu366Ter
ENST00000400525.6:c.1027G>T	ENSP00000383369.3:p.Glu343Ter
ENST00000462330.5:c.19G>T	ENSP00000485603.2:p.Glu7Ter
ENST00000462843.2:c.46G>T	ENSP00000485466.2:p.Glu16Ter
ENST00000474308.5:c.1039G>T	ENSP00000485665.1:p.Glu347Ter
ENST00000485358.5:c.64G>T	ENSP00000485499.2:p.Glu22Ter
ENST00000487165.5:n.1190G>T
ENST00000494454.5:n.1170G>T
ENST00000495655.2:n.640G>T
ENST00000542719.6:c.808G>T	ENSP00000485128.2:p.Glu270Ter
ENST00000634471.1:n.244-437G>T
ENST00000634537.1:c.325G>T	ENSP00000489208.1:p.Glu109Ter
NM_006440.4:c.1096G>T	NP_006431.2:p.Glu366Ter
NM_001352300.1:c.1093G>T	NP_001339229.1:p.Glu365Ter
NM_001352301.1:c.1006G>T	NP_001339230.1:p.Glu336Ter
NM_001352302.1:c.808G>T	NP_001339231.1:p.Glu270Ter
NR_147957.1:n.1228G>T
NM_006440.5:c.1096G>T MANE Select	NP_006431.2:p.Glu366Ter
NM_001352300.2:c.1093G>T	NP_001339229.1:p.Glu365Ter
NR_147957.2:n.1054G>T
NM_001352301.2:c.1006G>T	NP_001339230.1:p.Glu336Ter
NM_001352302.2:c.808G>T	NP_001339231.1:p.Glu270Ter